Articles | Volume 34, issue 1
https://doi.org/10.5194/ejm-34-35-2022
© Author(s) 2022. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
https://doi.org/10.5194/ejm-34-35-2022
© Author(s) 2022. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
The influence of oxygen fugacity and chlorine on amphibole–liquid trace element partitioning at upper-mantle conditions
Dipartimento di Scienze della Terra “A. Desio”, Università di
Milano, Via S. Botticelli 23, 20133 Milano, Italy
Massimo Tiepolo
Dipartimento di Scienze della Terra “A. Desio”, Università di
Milano, Via S. Botticelli 23, 20133 Milano, Italy
Giulio Borghini
Dipartimento di Scienze della Terra “A. Desio”, Università di
Milano, Via S. Botticelli 23, 20133 Milano, Italy
Antonio Langone
Istituto di Geoscienze e Georisorse, CNR, Via Ferrata 1, 27100 Pavia,
Italy
Patrizia Fumagalli
Dipartimento di Scienze della Terra “A. Desio”, Università di
Milano, Via S. Botticelli 23, 20133 Milano, Italy
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Detailed knowledge of the mechanisms ruling water incorporation in amphibole is essential to understand how much water can be fixed at upper-mantle conditions by this mineral. We provide the experimental evidence of the Cl effect on the oxo-substitution and the incorporation of water in amphibole. Finally, we highlight the versatility of confocal micro-Raman spectroscopy as an analytical tool to quantify water in amphibole.
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Lennart Koch and Burkhard C. Schmidt
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Volatile diffusivities in silicate melts control the nucleation and growth of bubbles in ascending magma. We investigated the diffusion of CO2 in an anhydrous and hydrous leucititic melt at high temperatures and high pressure. CO2 diffusion profiles were measured via attenuated total reflection Fourier transform infrared spectroscopy. CO2 diffusion increases with increasing temperature and water content. The data can be used to understand the CO2 degassing behaviour of leucititic melts.
Melanie J. Sieber, Max Wilke, Oona Appelt, Marcus Oelze, and Monika Koch-Müller
Eur. J. Mineral., 34, 411–424, https://doi.org/10.5194/ejm-34-411-2022, https://doi.org/10.5194/ejm-34-411-2022, 2022
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Carbonates reduce the melting point of the mantle, and carbonate melts produced in low-degree melting of a carbonated mantle are considered the precursor of CO2-rich magmas. We established experimentally the melting relations of carbonates up to 9 GPa, showing that Mg-carbonates melt incongruently to periclase and carbonate melt. The trace element signature of carbonate melts parental to kimberlites is approached by melting of Mg-rich carbonates.
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Carla Tiraboschi, Francesca Miozzi, and Simone Tumiati
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This review provides an overview of ex situ carbon-saturated COH fluid experiments at upper-mantle conditions. Several authors experimentally investigated the effect of COH fluids. However, fluid composition is rarely tackled as a quantitative issue, and rather infrequently fluids are analyzed as the associated solid phases in the experimental assemblage. Recently, improved techniques have been proposed for analyses of COH fluids, leading to significant advancement in fluid characterization.
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Detailed knowledge of the mechanisms ruling water incorporation in amphibole is essential to understand how much water can be fixed at upper-mantle conditions by this mineral. We provide the experimental evidence of the Cl effect on the oxo-substitution and the incorporation of water in amphibole. Finally, we highlight the versatility of confocal micro-Raman spectroscopy as an analytical tool to quantify water in amphibole.
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How, and how fast, does hydrogen move through crystals? We consider this question by adding hydrogen, by diffusion, to synthetic crystals of olivine doped with trace amounts of chromium. Even in a highly simplified system, the behaviour of hydrogen is complex. Hydrogen can move into and through the crystal using various pathways (different defects within the crystal) and hop between these pathways too.
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Grain boundary diffusion is orders of magnitude faster compared to volume diffusion. We studied this fast transport process in a well-defined garnet grain boundary. State-of-the-art microscopy was used for quantification. A dedicated numerical diffusion model shows that iron diffusion requires the operation of two diffusion modes, one fast, one slow. We conclude that impurity bulk diffusion in garnet aggregates is always dominated by grain boundary diffusion.
Giulio Borghini and Patrizia Fumagalli
Eur. J. Mineral., 32, 251–264, https://doi.org/10.5194/ejm-32-251-2020, https://doi.org/10.5194/ejm-32-251-2020, 2020
Alan B. Woodland, Andrei V. Girnis, Vadim K. Bulatov, Gerhard P. Brey, and Heidi E. Höfer
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We experimentally explored direct entrapment of breyite (CaSiO3) by diamond at upper-mantle conditions in a model subducted sediment rather than formation by retrogression of CaSiO3 perovskite, implying a deeper origin. Anhydrous low-T melting of CaCO3+SiO2 precludes breyite formation. Under hydrous conditions, reduction of melt results in graphite with breyite. Thus, breyite inclusions in natural diamond may form from aragonite + coesite or carbonate melt at 6–8 GPa via reduction with water.
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Short summary
Amphibole–liquid partitioning of elements of geological relevance is experimentally derived at conditions compatible with those of the Earth's upper mantle. Experiments are carried out at different oxygen fugacity conditions and variable Cl content in order to investigate their influence on the amphibole–liquid partition coefficients. Our results point to the capability of amphibole to act as filter for trace elements at upper-mantle conditions, oxidized conditions, and Cl-rich environments.
Amphibole–liquid partitioning of elements of geological relevance is experimentally derived at...